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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210612Generated: November 3, 2026

Methacrylic Acid → Benzophenone

https://huagongshe.com/reaction/2210612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacrylic AcidHCID 4093—
Reactant4-HydroxybenzophenoneHCID 14347—
ReactantTetrabutylammonium HydroxideHCID 2723671—
SolventIsopropanolHCID 3776—
ProductBenzophenoneHCID 3102—
ProductMethacrylateHCID 87595—

Reaction Steps

In the following example, a terpolymer derivative having 0.88 mole % methacrylate and 0.07 mole % benzophenone (graft ratio 92.7%:7.3% methacrylate:benzophenone) was prepared by a procedure to Example A-3 except that the tetrabutylammonium salt was prepared by charging 101.3 mL tetrabutylammonium hydroxide (1.0 M in methanol), 8.3 g (8.2 mL) methacrylic acid, 1.01 g 4-hydroxybenzophenone, and 100 mL isopropanol to a second flask and stirring at room temperature to give a translucent yellowish solution. This mixture was then added to the polymeric cement, as in Example 4. The polymer was isolated by precipitation in isopropanol with 0.1% BHT stabilizer optionally added. 1HNMR (400 MHz, CDCl3) analysis confirmed 97.3% conversion of benzylic bromide to grafted species. These results are given in Table A.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05459174
Source datasetuspto-grants-1995_10
ORD IDord-73f4fa953e8c490a85e2ecc50c7c54b2
Source noteuspto-grants-1995_10